Impact of Cationic Surfactant on the Self-Assembly of Sodium Caseinate

2014 ◽  
Vol 62 (34) ◽  
pp. 8543-8554 ◽  
Author(s):  
Marko Vinceković ◽  
Marija Ćurlin ◽  
Darija Jurašin
2017 ◽  
Vol 64 ◽  
pp. 1-8 ◽  
Author(s):  
Peggy Thomar ◽  
Alberto Gonzalez-Jordan ◽  
Jens Dittmer ◽  
Taco Nicolai

2021 ◽  
pp. 118012
Author(s):  
Yingbiao Xu ◽  
Jinyong Song ◽  
Tingyi Wang ◽  
Mingming Xu ◽  
Lingyu Zhang ◽  
...  

Data in Brief ◽  
2018 ◽  
Vol 16 ◽  
pp. 276-285
Author(s):  
Yaqiong Zhang ◽  
Puyu Yang ◽  
Fangyi Yao ◽  
Jie Liu ◽  
Liangli (Lucy) Yu

Langmuir ◽  
2014 ◽  
Vol 30 (39) ◽  
pp. 11493-11503 ◽  
Author(s):  
Ana Maria Percebom ◽  
Leandro Ramos Souza Barbosa ◽  
Rosangela Itri ◽  
Watson Loh

Soft Matter ◽  
2019 ◽  
Vol 15 (25) ◽  
pp. 5052-5059 ◽  
Author(s):  
Hongyao Yin ◽  
Fuxing Zhan ◽  
Yue Yu ◽  
Zongcheng Li ◽  
Yujun Feng ◽  
...  

Hydrophilic honeycomb films are directly fabricated by the self-assembly of complexes of polylacticacid and dodecyl trimethyl ammonium chloride in ‘breath figure’ templating. The presence of a cationic surfactant not only improves film regularity, but also imparts them with excellent wettability.


2014 ◽  
Vol 26 (24) ◽  
pp. 7183-7188 ◽  
Author(s):  
Bhupendra K. Singh ◽  
Dongdong Xu ◽  
Lu Han ◽  
Jian Ding ◽  
Yimeng Wang ◽  
...  

1999 ◽  
Vol 9 (3-6) ◽  
pp. 281-286 ◽  
Author(s):  
Donald Farrer ◽  
Alex Lips

Author(s):  
M. Kessel ◽  
R. MacColl

The major protein of the blue-green algae is the biliprotein, C-phycocyanin (Amax = 620 nm), which is presumed to exist in the cell in the form of distinct aggregates called phycobilisomes. The self-assembly of C-phycocyanin from monomer to hexamer has been extensively studied, but the proposed next step in the assembly of a phycobilisome, the formation of 19s subunits, is completely unknown. We have used electron microscopy and analytical ultracentrifugation in combination with a method for rapid and gentle extraction of phycocyanin to study its subunit structure and assembly.To establish the existence of phycobilisomes, cells of P. boryanum in the log phase of growth, growing at a light intensity of 200 foot candles, were fixed in 2% glutaraldehyde in 0.1M cacodylate buffer, pH 7.0, for 3 hours at 4°C. The cells were post-fixed in 1% OsO4 in the same buffer overnight. Material was stained for 1 hour in uranyl acetate (1%), dehydrated and embedded in araldite and examined in thin sections.


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